美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA075541"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
42806-038-01 42806-038 HUMAN PRESCRIPTION DRUG Betaxolol Betaxolol TABLET, FILM COATED ORAL 20100720 N/A ANDA ANDA075541 Epic Pharma LLC BETAXOLOL HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (42806-038-01)
42806-038-10 42806-038 HUMAN PRESCRIPTION DRUG Betaxolol Betaxolol TABLET, FILM COATED ORAL 20100720 N/A ANDA ANDA075541 Epic Pharma LLC BETAXOLOL HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (42806-038-10)
42806-039-01 42806-039 HUMAN PRESCRIPTION DRUG Betaxolol Betaxolol TABLET, FILM COATED ORAL 20100720 N/A ANDA ANDA075541 Epic Pharma LLC BETAXOLOL HYDROCHLORIDE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (42806-039-01)
42806-039-10 42806-039 HUMAN PRESCRIPTION DRUG Betaxolol Betaxolol TABLET, FILM COATED ORAL 20100720 N/A ANDA ANDA075541 Epic Pharma LLC BETAXOLOL HYDROCHLORIDE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (42806-039-10)
24658-700-01 24658-700 HUMAN PRESCRIPTION DRUG Betaxolol Betaxolol TABLET, FILM COATED ORAL 20161215 N/A ANDA ANDA075541 PuraCap Laboratories LLC BETAXOLOL HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (24658-700-01)
24658-701-01 24658-701 HUMAN PRESCRIPTION DRUG Betaxolol Betaxolol TABLET, FILM COATED ORAL 20161215 N/A ANDA ANDA075541 PuraCap Laboratories LLC BETAXOLOL HYDROCHLORIDE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (24658-701-01)
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